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Research Paper
Clinical and genetic characteristics of myotonia congenita in Chinese population
Yuting Hea Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Yusen Qiua Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;b Rare Disease Center, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Ying Xionga Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;b Rare Disease Center, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Yu Shena Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Kaiyan Jianga Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Hancun Yia Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Pengcheng Huanga Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Yu Zhua Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;b Rare Disease Center, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Min Zhua Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;b Rare Disease Center, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Meihong Zhoua Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;b Rare Disease Center, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, ChinaView further author information
, Daojun Honga Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;b Rare Disease Center, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;c Institute of Neurology, Jiangxi Academy of Clinical Medical Science, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;d Key Laboratory of Rare Neurological Diseases of Jiangxi Provincial Health Commission, Jiangxi Medical College, Nanchang University, Nanchang, ChinaCorrespondence[email protected]
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Dandan Tana Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;b Rare Disease Center, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;c Institute of Neurology, Jiangxi Academy of Clinical Medical Science, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China;d Key Laboratory of Rare Neurological Diseases of Jiangxi Provincial Health Commission, Jiangxi Medical College, Nanchang University, Nanchang, ChinaCorrespondence[email protected]
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Article: 2349823
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Received 15 Nov 2023, Accepted 22 Mar 2024, Published online: 08 May 2024
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